Canonical Allele Identifier: CA359196713

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13708288G>T (hg19) ; chr5:g.13708179G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13708179G>T , CM000667.2:g.13708179G>T	GRCh38
NC_000005.9:g.13708288G>T , CM000667.1:g.13708288G>T	GRCh37
NC_000005.8:g.13761288G>T	NCBI36
NG_013081.1:g.241302C>A
NG_013081.2:g.241302C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.615C>A
ENST00000265104.5:c.13282C>A MANE Select	ENSP00000265104.4:p.Leu4428Met
ENST00000681290.1:c.13237C>A	ENSP00000505288.1:p.Leu4413Met
ENST00000265104.4:c.13282C>A	ENSP00000265104.4:p.Leu4428Met
NM_001369.2:c.13282C>A	NP_001360.1:p.Leu4428Met
XM_005248262.2:c.13237C>A	XP_005248319.1:p.Leu4413Met
XM_005248262.3:c.13390C>A	XP_005248319.2:p.Leu4464Met
XM_017009177.1:c.12970C>A	XP_016864666.1:p.Leu4324Met
XM_017009178.1:c.12295C>A	XP_016864667.1:p.Leu4099Met
XM_017009179.2:c.12295C>A	XP_016864668.1:p.Leu4099Met
XM_017009185.1:c.8479C>A	XP_016864674.1:p.Leu2827Met
XM_017009186.1:c.8032C>A	XP_016864675.1:p.Leu2678Met
XM_017009188.1:c.7369C>A	XP_016864677.1:p.Leu2457Met
XM_024454388.1:c.12295C>A	XP_024310156.1:p.Leu4099Met
XM_024454389.1:c.11884C>A	XP_024310157.1:p.Leu3962Met
NM_001369.3:c.13282C>A MANE Select	NP_001360.1:p.Leu4428Met